Latest recalls — page 43
Older notices, newest first.
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NHTSA safety recall · 2 months ago
Mitsubishi Outlander and Outlander PHEV recall: Due to improper software programming, the Alliance In-Vehicle Infotainment
Due to improper software programming, the Alliance In-Vehicle Infotainment (A-IVI) system may fail to display the rearview camera image when the…
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NHTSA safety recall · 2 months ago
Ford Mustang recall: The engine compartment wiring harness ground connections may fracture
The engine compartment wiring harness ground connections may fracture and result in a loss of drive power, or a loss of function in the windshield…
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NHTSA safety recall · 2 months ago
Kia EV9 recall: Due to improper routing, the Occupant Detection System (ODS)
Due to improper routing, the Occupant Detection System (ODS) may not deactivate the air bag when a child or child seat is in the front passenger…
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NHTSA safety recall · 2 months ago
Marathon Industries recall: The deck pins may break, resulting in the liftgate platform falling
The deck pins may break, resulting in the liftgate platform falling.
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NHTSA safety recall · 2 months ago
General recall: The rearview camera screen may display a distorted or blank image
The rearview camera screen may display a distorted or blank image.
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Highest risk · 2 months ago
Workbless Electric Pressure Washers recall: The recalled pressure washers lack an integral ground-fault
The recalled pressure washers lack an integral ground-fault circuit-interrupter (GFCI) and an adequate-length power cord, posing serious risks of…
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Highest risk · 2 months ago
Modine Manufacturing Company Airedale Heating and Cooling Ventilation Fans recall: Fire Hazard
Fire Hazard
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Highest risk · 2 months ago
KTM North America Off-Road Motorcycles recall: Risk of Serious Injury or Death from Crash Hazard
Risk of Serious Injury or Death from Crash Hazard
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Highest risk · 2 months ago
Dreams Bedding Technology PTE. Ltd. Koorlian Mattresses recall: The recalled mattresses violate the mandatory flammability standard
The recalled mattresses violate the mandatory flammability standard for mattresses, posing a risk of serious injury or death from fire.
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Highest risk · 2 months ago
Jinhezo Mini Waterproof LED Tea Lights recall: The LED Tea Lights violate the mandatory safety standard for consumer
The LED Tea Lights violate the mandatory safety standard for consumer products with button cell and coin batteries because the button batteries can…
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Highest risk · 2 months ago
Goal Zero YETI 3000X Power Stations recall: Serious Risk of Injury from Fire and Burn Hazards
Serious Risk of Injury from Fire and Burn Hazards
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Highest risk · 2 months ago
CCM Hockey U.S. Fmhvr Hybrid Visors and Acchvr Replacement Visor Accessories recall: Risk of Injury from Laceration or Impact Hazards
Risk of Injury from Laceration or Impact Hazards
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Class II · 2 months ago
Philips Azurion Rystem, Model Numbers: 722063, 722064, 722067 recall: Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential
Two software related issues affecting Azurion R2.2.10 Systems: 1) Potential image quality degradation that may lead to delay of therapy, procedural…
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Class II · 2 months ago
Biofire Respiratory Panel 2.1 REF 423742 UDI code: 00815381020529 recall: Due to increase in false negative results
Due to increase in false negative results
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Class II · 2 months ago
OBP Medical , ER-Spec Single-Use Vaginal Speculum with LED Light recall: There is a potential for vaginal speculums to contain a burr on the proximal
There is a potential for vaginal speculums to contain a burr on the proximal plastic blade, which may introduce a sharp edge in the contact regions…
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Class II · 2 months ago
Covidien, LP Dermalon 88861757-31 Dermalon* 4-0 BLU 75CM C13 88861757-31 88861799-31 recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
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Class II · 2 months ago
Cardinal Health Presource Kits: 1) Basic Pack recall: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
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Class II · 2 months ago
Covidien, LP Surgipro SP-623 Surgipro* 2-0 BLU 75CM SC2 X36 SP-623 recall: Product may contain a perforation or tear in the sterile barrier packaging
Product may contain a perforation or tear in the sterile barrier packaging. This issue may result in biocontamination of the sterile sutures, which…
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Class II · 2 months ago
Bioporto Diagnostics A/S ProNephro AKI Reagent Kit . IVD Acute Kidney Injury Test recall: The use of a non-validated rework process for assay reagents which could lead
The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment…
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Class II · 2 months ago
Straumann USA LLC GM Helix Implant, Endosseous Dental Implant Article No. 109.984 recall: There may be a mismatch between the implant contained inside the packaging
There may be a mismatch between the implant contained inside the packaging and the information described on the outer carton label. If the the…
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Class II · 2 months ago
Cardinal Health Presource Kits: 1) Septo Rhino Pack recall: Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled
Procedure kits contain MEDICOM Ritmed Neurological Sponges that were recalled due to unexpected variability in endotoxin levels.
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Class II · 2 months ago
Waldemar Link GmbH & Co. KG Endo-Model, Replacement Set, Tibial Plateau, right/left, L recall: The affected Endo-Model replacement set for a Rotating Hinge tibial plateau
The affected Endo-Model replacement set for a Rotating Hinge tibial plateau incorrectly contains a Pure Hinge plateau. The incorrect plateau could…
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Class II · 2 months ago
Bd Switzerland Sarl 60 In Non-DEHP Minibore Extension Set RES ME2010 UDI-DI code recall: Products may not have received adequate sterilization processing
Products may not have received adequate sterilization processing.
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Class II · 2 months ago
Spacelabs Healthcare, Inc. Brand Name: Xhibit Product Name: Xhibit Central Station recall: Due to off-the-shelf display port component that has audio/video failures
Due to off-the-shelf display port component that has audio/video failures